Funded Pilot and Feasibility Study #2:Title: Glycosaminoglycan reactivity in lupus as a predictor of diseasePI: Fei Shih, M.D., Ph.D.A.
Specific Aims Systemic lupus erythematosus (SLE) is characterized by the production of autoantibodies andautoimmune attack of multiple organs. We hypothesized that there are novel targets yet to bediscovered for SLE and these may serve as predictors of disease. Based on the highly patternedstructure of DNA, we hypothesized that cross reactivity to glycosaminoglycans (GAGs), also a highlypatterned structure, may serve as a biomarker for various disease manifestations. This pilot studyexamines aGAG reactivity in a murine model of SLE and extends aGAG analysis to pediatricpatients with SLE with the following specific aims: 1) An unbiased examination of aGAG antibodiesin KRN/G7m mice, a murine model of SLE; and 2) Characterize aGAG antibodies in SLE patientsand correlation with disease.

Agency
National Institute of Health (NIH)
Institute
National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)
Type
Center Core Grants (P30)
Project #
5P30AR048335-08
Application #
7680340
Study Section
Special Emphasis Panel (ZAR1-EHB-D (O1))
Project Start
2008-09-01
Project End
2011-08-31
Budget Start
2008-09-01
Budget End
2009-08-31
Support Year
8
Fiscal Year
2008
Total Cost
$91,816
Indirect Cost
Name
Washington University
Department
Type
DUNS #
068552207
City
Saint Louis
State
MO
Country
United States
Zip Code
63130
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